Planta Med 2019; 85(18): 1483-1484
DOI: 10.1055/s-0039-3399883
Main Congress Poster
Poster Session 1
© Georg Thieme Verlag KG Stuttgart · New York

Flavonoids and oxepinones from the leaves and twigs of Desmos cochinchinensis and their α-glucosidase inhibitory activities

P Meesakul
1   1 Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University,, Chiang Rai 57100, Thailand
,
C Richardson
2   School of Chemistry and Molecular Biosciences, University of Wollongong,, Wollongong, New South Wales, 2522 Australia
,
SG Pyne
2   School of Chemistry and Molecular Biosciences, University of Wollongong,, Wollongong, New South Wales, 2522 Australia
,
S Laphookhieo
1   1 Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University,, Chiang Rai 57100, Thailand
› Author Affiliations
Further Information

Publication History

Publication Date:
20 December 2019 (online)

 

Desmos cochinchinensis, belonging to the Annonaceae family, is a shrub widely distributed in Asia. Several secondary metabolites including, terpenoids, alkaloids, chalcones, and flavonoids have been isolated from this plant. Some of these compounds showed useful biological properties including antitumor, anti-inflammatory, antiviral and anti-HIV activities. Herein, twenty-four compounds comprising four new flavonoids (14), a new benzyl benzoate derivative (5), five new oxepinones (610), and fourteen known compounds were isolated and purified from the twigs and leaves of D. cochinchinensis by various column chromatographic techniques. Their structures were established by spectroscopic methods. The structure of compound 1 was confirmed from X-ray diffraction data with Mo Kα radiation. The absolute configurations of 3, 4, and 610 were identified from comparisons of their ECD spectra with those reported compounds. Compounds 1, 2, 6, 8, and 10 showed α-glucosidase inhibitory activities with IC50 values of 0.2, 0.2, 3.6, 4.9, and 3.1 µM, respectively, which were better than the positive control, acarbose, (IC50 170.7 µM).

Zoom Image
Fig. 1